School of Pharmacy and Life Sciences, Robert Gordon University, Aberdeen AB10 7GJ, UK.
School of Pharmacy and Life Sciences, Robert Gordon University, Aberdeen AB10 7GJ, UK.
Sci Total Environ. 2022 Feb 20;808:152071. doi: 10.1016/j.scitotenv.2021.152071. Epub 2021 Dec 2.
It is proposed that microplastics discharged from wastewater treatment plants act as a vector of pharmaceuticals. In this study, adsorption of pharmaceuticals to polyethylene microplastics was investigated in municipal wastewater. Pharmaceuticals for study were selected to represent different speciation (anionic, cationic, and neutral) and a range of pH dependant octanol-water distribution coefficients (log D). Findings revealed adsorption favoured those in cationic form with the greatest hydrophobicity (e.g., fluoxetine log D 2.0 at pH 7.8). Adsorption of anionic pharmaceuticals was restricted due to repulsion with the microplastic's negatively charged surface. Only atorvastatin had any appreciable adsorption due to its comparatively high log D value (2.9). Those pharmaceuticals predominantly in neutral form (carbamazepine and ketamine) with log D values ≥2.4 had similar adsorption. Freundlich K values were 3400, 386, 284, 259 and 218 (mg kg)(mg L) for fluoxetine, propranolol, atorvastatin, ketamine, and carbamazepine, respectively. All pharmaceuticals with log D values <1.0 (atenolol, gliclazide, bezafibrate, and ifosfamide) did not adsorb to microplastics, irrespective of their speciation. Changing composition of wastewater (pH, dilution with stormwater and NaCl addition) within the range expected for municipal wastewater had limited influence on adsorption. Pharmaceutical desorption from microplastics was assessed in river water and simulated gastric and intestinal fluids. Solution pH was considered the most important factor for pharmaceutical desorption, influencing both pharmaceutical speciation and microplastic surface charge. Greatest desorption was observed for the cationic pharmaceuticals in gastric fluids due to a reduced surface charge of the microplastics under low pH conditions. Up to 50% desorption of fluoxetine occurred in gastric fluid at 37 °C. These findings show that pharmaceuticals adsorbed to microplastics are 'bioavailable'. However, this is often overlooked as an exposure route to aquatic organisms because water samples are normally pre-filtered prior to chemical analysis.
有人提出,污水处理厂排放的微塑料可以作为药物的载体。在这项研究中,研究了药物在城市废水中对聚乙烯微塑料的吸附。选择用于研究的药物代表不同的形态(阴离子、阳离子和中性)和一系列依赖 pH 值的辛醇-水分配系数(log D)。研究结果表明,吸附有利于那些具有最大疏水性的阳离子形式的药物(例如,氟西汀在 pH 7.8 时的 log D 为 2.0)。由于与微塑料带负电荷的表面相互排斥,阴离子药物的吸附受到限制。只有阿托伐他汀由于其相对较高的 log D 值(2.9)才有明显的吸附。那些主要以中性形式存在(卡马西平和氯胺酮)且 log D 值≥2.4 的药物具有相似的吸附。对于氟西汀、普萘洛尔、阿托伐他汀、氯胺酮和卡马西平,弗伦德利希 K 值分别为 3400、386、284、259 和 218(mg kg)(mg L)。所有 log D 值<1.0(阿替洛尔、格列齐特、贝扎贝特和异环磷酰胺)的药物都不会吸附到微塑料上,无论它们的形态如何。在城市废水中预期的范围内,改变废水的组成(pH 值、与暴雨的稀释和 NaCl 的添加)对吸附的影响有限。在河水和模拟胃液及肠液中评估了药物从微塑料上的解吸。溶液 pH 值被认为是影响药物形态和微塑料表面电荷的药物解吸的最重要因素。在低 pH 条件下,由于微塑料表面电荷降低,阳离子药物在胃液中观察到最大的解吸。在 37°C 时,氟西汀在胃液中有多达 50%的解吸。这些发现表明,吸附在微塑料上的药物是“生物可利用的”。然而,由于水样在进行化学分析之前通常要预先过滤,因此这通常被忽视为水生生物的暴露途径。